Patrick Short
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
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- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- Epigenetics and DNA Methylation
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 6
-
- CRISPR and Genetic Engineering 1
- Amyloidosis: Diagnosis, Treatment, Outcomes 1
- Co-authors
- Matthew E. Hurles (4 shared papers)Giuseppe Gallone (3 shared papers)Helen Firth (3 shared papers)Jeremy F. McRae (2 shared papers)David R FitzPatrick (3 shared papers)Alejandro Sifrim (2 shared papers)Lewis E. Vogler (1 shared paper)K. A. JUN. NORTON (1 shared paper)
- Journals
- Nature (4 papers)Nature Communications (2 papers)Science (1 paper)Nature Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesJapan
In The Last Decade
Patrick Short
15 papers receiving 1.5k citations
Patrick Short's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 746
- Molecular Biology 674
- Cancer Research 107
- Health Information Management 20
- Cognitive Neuroscience 83
Countries citing papers authored by Patrick Short
This map shows the geographic impact of Patrick Short's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Patrick Short with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Short more than expected).
Fields of papers citing papers by Patrick Short
This network shows the impact of papers produced by Patrick Short. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Patrick Short. The network helps show where Patrick Short may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Short, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 402 |
| 2 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 395 |
| 3 | 2018 | 176 | |
| 4 | 2018 | 146 | |
| 5 | 2012 | 101 | |
| 6 | 1955 | 66 | |
| 7 | 1995 | 61 | |
| 8 | 2022 | 61 | |
| 9 | 2015 | 51 | |
| 10 | 2019 | 40 | |
| 11 | 2020 | 18 | |
| 12 | 2025 | 13 | |
| 13 | 2023 | 9 | |
| 14 | 2023 | 6 | |
| 15 | 2019 | 2 |
About Patrick Short
Patrick Short is a scholar working on Genetics, Molecular Biology, Cancer Research, Health Information Management and Nephrology, having authored 15 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), CRISPR and Genetic Engineering (1 paper), Cancer Genomics and Diagnostics (1 paper), Chronic Kidney Disease and Diabetes (1 paper), Prenatal Screening and Diagnostics (1 paper), Renal Diseases and Glomerulopathies (1 paper) and Amyloidosis: Diagnosis, Treatment, Outcomes (1 paper). The work is most often cited by research in Genetics (746 citations), Molecular Biology (674 citations), Cancer Research (107 citations), Health Information Management (20 citations) and Cognitive Neuroscience (83 citations). Patrick Short has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Matthew E. Hurles, Giuseppe Gallone, Helen Firth, Jeremy F. McRae, David R FitzPatrick, Alejandro Sifrim, Lewis E. Vogler, K. A. JUN. NORTON, William M. Mansfield and Jeffrey C. Barrett. Their work appears in journals such as Nature, Nature Communications, Science, Nature Genetics and Journal of Medical Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.